Centre for Biological Timing, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Methods Mol Biol. 2021;2130:249-262. doi: 10.1007/978-1-0716-0381-9_19.
The discovery of the suprachiasmatic nucleus (SCN) as the master mammalian pacemaker has since opened up a variety of alternative methods for assessing how external timing cues influence the clock. One powerful approach for understanding how sensory inputs influence the SCN is to monitor acute changes in SCN electrophysiological activity via in vivo extracellular recording. This methodology offers the ability to monitor stimulus-evoked changes in SCN function at very fine timescales and to rapidly test multiple stimuli and/or stimulus repeats within a single animal. In this chapter we describe our methods for acute in vivo multielectrode recording in head-fixed, anesthetized rodents. These allow for monitoring of single-cell/population activity for >12 h; enable the delivery of carefully controlled sensory stimuli; can be used alongside an array of established or novel experimental tools; and are easily adapted to study activity in any other brain region.
作为主生物钟的视交叉上核 (SCN) 的发现,为评估外部时间线索如何影响生物钟提供了各种替代方法。了解感觉输入如何影响 SCN 的一种强大方法是通过活体细胞外记录来监测 SCN 电生理活动的急性变化。这种方法能够在非常精细的时间尺度上监测 SCN 功能的刺激诱发变化,并在单个动物中快速测试多种刺激和/或刺激重复。在本章中,我们描述了在头部固定、麻醉啮齿动物中进行急性活体多电极记录的方法。这些方法允许对单细胞/群体活动进行 >12 小时的监测;能够提供精心控制的感觉刺激;可与一系列已建立或新颖的实验工具一起使用;并且易于适应研究任何其他脑区的活动。